A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053363



Internal ID19142582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:104877606..105237012hg38UCSC Ensembl
Innerchr13:105529957..105889363hg19UCSC Ensembl
Innerchr13:104327958..104687364hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38359407
hg19359407
hg18359407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1738n100
Supporting Variantsnssv3525555
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053363
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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